Study of reactions leading to sulfine formation. 4. Evidence for a reversible E1cB mechanism for base-induced elimination of N,N-diisopropyl-9-fluorenesulfinamide
Author:
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo00292a028
Cited by 7 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Synthesis of Carbamates from Diethoxycarbonyl Hydrazine Derivatives by E1cB Eliminative Cleavage of the N−N′-Bond Rather than Reduction;Organic Letters;2009-11-12
2. Kinetics and mechanism of hydrolysis of N-amidomethylsulfonamides;Journal of the Chemical Society, Perkin Transactions 2;2001
3. Nucleophilic substitution in benzylic thiophosphinyl and thiophosphonyl chlorides: the contribution of elimination–addition pathways with methylenethioxophosphorane (thiophosphene) intermediates;J. Chem. Soc., Perkin Trans. 2;1994
4. A novel synthesis of monosubstituted sulfines via an unusual β-elimination of chloroform from allylic and benzylic trichloromethyl sulfoxides;Tetrahedron Letters;1994-01
5. Theoretical investigation on base-induced 1,2-eliminations in the model system fluoride ion + fluoroethane. The role of the base as a catalyst;Journal of the American Chemical Society;1993-10
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